Kubota T, Chiba K
Research Testing Department, SRL, Inc., Hachioji-shi, Tokyo, Japan.
Br J Clin Pharmacol. 2001 May;51(5):475-7. doi: 10.1046/j.1365-2125.2001.01371.x.
To determine the frequencies of four thiopurine S-methyltransferase (TPMT) mutant alleles, TPMT*2, *3A, *3B and *3C in a normal Japanese population.
Genotypes were determined in 151 Japanese subjects and in six family members of a propositus using polymerase chain reaction (PCR)-restriction fragment length polymorphism and allele-specific PCR assays.
Only one TPMT3C heterozygote was identified (gene frequency 0.3%). TPMT2, *3A and 3B were not detected. In addition, TPMT3C was found to have been inherited from the mother and passed on to the son of the propositus.
TPMT*3C appears to be most prevalent among the known mutant allele of TPMT in a Japanese population which may have some relevance for the treatment of Japanese patients with thiopurine drugs.
确定正常日本人群中四种硫嘌呤甲基转移酶(TPMT)突变等位基因TPMT*2、*3A、3B和3C的频率。
采用聚合酶链反应(PCR)-限制性片段长度多态性和等位基因特异性PCR检测法,对151名日本受试者及一名先证者的六名家庭成员进行基因分型。
仅鉴定出一名TPMT3C杂合子(基因频率0.3%)。未检测到TPMT2、3A和3B。此外,发现TPMT*3C是从母亲遗传而来,并传递给了先证者的儿子。
在日本人群中,TPMT*3C似乎是TPMT已知突变等位基因中最常见的,这可能与日本硫嘌呤类药物治疗患者有关。